HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyl-2-butanol → HCID 44623807, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyl-2-butanol | HCID 6405 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(6-Bromopyridin-2-yl)acetonitrile | HCID 642864 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | 5-Amino-2-[4-(1-hydroxy-1-methylethyl)phenyl]-1,3-thiazole-4-carboxamide | HCID 58335264 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | HCID 44623807 | HCID 44623807 | — |
Reaction Steps
The title compound was prepared as described in Example 1, Step 2 using 5-amino-2-[4-(1-hydroxy-1-methylethyl)phenyl]-1,3-thiazole-4-carboxamide (Example 5, Step 3) (150 mg, 0.54 mmol), (6-bromopyridin-2-yl)acetonitrile (107 mg, 0.54 mmol), Pd2(dba)3 (30 mg, 0.032 mmol), X-PHOS (77 mg, 0.16 mmol), potassium carbonate (82 mg, 0.60 mmol), and tert-amyl alcohol (1.2 ml) as starting materials. 1H NMR (600 MHz, d6-DMSO) δ 11.31 (s, 1H), 7.86 (d, 2H), 7.73 (m, 2H), 7.62 (s, 1H), 7.53 (d, 2H), 7.16 (d, 1H), 6.94 (d, 1H), 5.08 (s, 1H), 4.27 (s, 2H), 1.42 (s, 6H). LRMS (APCI) calc'd for C20H20N5O2S [M+H]+ 394.1, found 394.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08278335B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-64931a4ef5f24874a288252ae29235ce |
| Source note | uspto-grants-2012_10 |